|
771
|
|
|
Pleckstrin homology and RhoGEF domain containing G5 |
ARHGEF45, CMTRIC, DSMA4, GEF720, HMNR4, Syx, Tech |
Charcot-marie-tooth disease, Congenital clubfoot, Distal amyotrophy, Distal spinal muscular atrophy, Facioscapulohumeral spinal muscular atrophy, Distal hereditary motor neuronopathy, Multiple sclerosis, Sclerocystic ovaries, Polycystic ovary syndrome, Scoliosis, Spinal muscular atrophy |
|
772
|
|
|
Parathyroid hormone 1 receptor |
EKNS, PFE, PTHR, PTHR1 |
Cubitus valgus, Anemia, Aortic coarctation, Blomstrand lethal chondrodysplasia, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Cataract, Choanal atresia, Chondrodysplasia punctata, Chondrosarcoma, Pulmonary hypoplasia, Diabetes mellitus, Dwarfism, Dyschondroplasias, Eiken skeletal dysplasia, Eiken syndrome, Enchondromatosis, Epiphyseal dysplasia, Failure of tooth eruption, Hip contracture, Hydrops fetalis, Hypercalcemia, Hyperparathyroidism, Hypodontia, Hypoparathyroidism, Laryngeal calcification, Liver carcinoma, Lung diseases, Lymphangioma, Mesomelia, Metaphyseal chondrodysplasia, Micrognathism, Micromelia, Nephrocalcinosis, Ollier disease, Osseous ankylosis, Osteochondrodysplasia, Osteopenia, Osteosclerosis, Phosphate diabetes, Precocious puberty, Proptosis, Rhizomelia, Rickets, Sacral agenesis, Skeletal dysplasia, Spade-like hand, Talipes transversoplanus, Visceral angiomatosisView all (35 more) |
|
773
|
|
|
Parathyroid hormone 2 receptor |
PTHR2 |
|
|
774
|
|
|
Protein tyrosine kinase 2 |
FADK, FADK 1, FAK, FAK1, FRNK, PPP1R71, p125FAK, pp125FAK |
Atrial fibrillation, Carcinoma, Giant cell glioblastoma, Glioblastoma, Liver carcinoma, Metastatic melanoma, Mouth neoplasms, Malignant neoplasm of mouth, Non-obstructive azoospermia, Paroxysmal atrial fibrillation, Rheumatoid arthritis |
|
775
|
|
|
Proline rich 12 |
KIAA1205, NOC |
Autism, Developmental delay, Dysmorphic features, Esotropia, Exotropia, Hearing loss, Lupus erythematosus, Mental retardation, Myositis, Ptosis, Rheumatoid arthritis, Scleroderma |
|
776
|
|
|
Pleckstrin homology and RhoGEF domain containing G1 |
ARHGEF41 |
|
|
777
|
|
|
Protocadherin 19 |
DEE9, EFMR, EIEE9 |
Absence seizure, Anxiety disorder, Autism, Bilateral convulsive seizures, Clonic seizures, Developmental delay, Developmental regression, Dravet syndrome, Dyscognitive seizures, Dysmorphic features, Epilepsy, Epileptic encephalopathy and intellectual disability, Febrile seizures, Female restricted epilepsy with intellectual disability, Focal clonic seizures, Focal seizures, Hypotonic seizures, Mental retardation, Motor delay, Myoclonic epilepsy, Myoclonic seizures, Obsessive-compulsive disorder, Obtundation status, Psychosis, Seizure, Status epilepticus, Strabismus, Temporal cortical atrophyView all (13 more) |
|
778
|
|
|
Protein tyrosine kinase 7 (inactive) |
CCK-4, CCK4 |
|
|
779
|
|
|
Prothymosin alpha |
TMSA |
|
|
780
|
|
|
Protocadherin 10 |
OL-PCDH, PCDH19 |
|
